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dc.contributor.authorOwens, CL
dc.contributor.authorNash, GR
dc.contributor.authorHadler, K
dc.contributor.authorFitzpatrick, RS
dc.contributor.authorAnderson, CG
dc.contributor.authorWall, F
dc.date.accessioned2019-02-04T15:32:10Z
dc.date.issued2019-01-29
dc.description.abstractApatite subspecies depend on their halogen and hydroxyl content; chlorapatite, hydroxylapatite and fluorapatite, with additional substitution of other elements within the lattice such as rare earth elements (REE), sodium, strontium and manganese also possible. Rare earth elements are vital to green and emerging technologies, with demand set to outstrip supply. Apatite provides a possible future source of REE. Processing rare earth deposits is often complex, with surface behaviour having a significant effect on the optimization of a process flow sheet. The effect of enrichment of natural apatite and the doping of synthetic apatite on surface behaviour can be determined by measuring the zeta potential and the isoelectric point of the mineral. In this paper, we review zeta potential studies of natural and synthetic apatite to determine the effect of elemental enrichment on surface behaviour. Fifty three studies of natural apatite and forty four studies of synthetic apatite were reviewed. The isoelectric point of apatite varied from pH 1 to pH 8.7, with studies of apatite specified to be >90% pure reducing the variation to pH 3 to pH 6.5. Of the four studies of rare earth enriched apatite found, three had IEP values between pH 3 and pH 4. A study of synthetic apatite showing enrichment of between 1 and 10% by the REE europium does not affect surface behaviour. However, no studies were found that investigated the effect of common REE processing reagents on REE enriched apatite zeta potentials. Therefore, in addition to comparing previous studies we also therefore present new zeta potential measurements of apatite from a REE enriched deposit under water and common flotation collector conditions. The IEP value of this apatite under water conditions was at pH 3.6, shifting to <3.5 under both hydroxamic acid and betacol conditions. When compared to previous studies, the behaviour of REE enriched apatite under collector conditions is similar to non-REE apatite. This result could be important for future processing of apatite enriched with REE, and therefore global apatite and rare earth supply.en_GB
dc.description.sponsorshipNatural Environment Research Council (NERC)en_GB
dc.description.sponsorshipMkango Resources Ltd.en_GB
dc.description.sponsorshipKroll Institute for Extractive Metallurgy, Department of Metallurgy and Materials Engineering, Colorado School of Minesen_GB
dc.identifier.citationVol. 265, pp. 14 - 28en_GB
dc.identifier.doi10.1016/j.cis.2019.01.004
dc.identifier.grantnumberNE/M011429/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/35719
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.rights© 2019 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).en_GB
dc.titleApatite enrichment by rare earth elements: A review of the effects of surface propertiesen_GB
dc.typeArticleen_GB
dc.date.available2019-02-04T15:32:10Z
dc.identifier.issn0001-8686
dc.descriptionThis is the final published version. Available from Elsevier via the DOI in this record.en_GB
dc.identifier.journalAdvances in Colloid and Interface Scienceen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2019-01-21
exeter.funder::Natural Environment Research Council (NERC)en_GB
rioxxterms.funderNatural Environment Research Councilen_GB
rioxxterms.identifier.projectNE/M 011429/1en_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2019-01-29
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-02-04T13:47:10Z
refterms.versionFCDVoR
refterms.dateFOA2019-02-04T15:32:14Z
refterms.panelBen_GB
refterms.depositExceptionpublishedGoldOA
rioxxterms.funder.projectb33ee755-a700-495b-a5b1-faaa2988b9aden_GB


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© 2019 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's licence is described as © 2019 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).